Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4IDI3
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0016407 | acetyltransferase activity | 5 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016746 | acyltransferase activity | 3 | 9 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.721 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.692 |
CLV_PCSK_PC1ET2_1 | 199 | 201 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.511 |
DEG_APCC_DBOX_1 | 350 | 358 | PF00400 | 0.385 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.488 |
DEG_SPOP_SBC_1 | 84 | 88 | PF00917 | 0.498 |
DOC_ANK_TNKS_1 | 358 | 365 | PF00023 | 0.384 |
DOC_CYCLIN_yCln2_LP_2 | 76 | 82 | PF00134 | 0.499 |
DOC_MAPK_gen_1 | 162 | 170 | PF00069 | 0.379 |
DOC_MAPK_gen_1 | 292 | 300 | PF00069 | 0.446 |
DOC_PP1_RVXF_1 | 295 | 301 | PF00149 | 0.370 |
DOC_PP1_RVXF_1 | 56 | 63 | PF00149 | 0.519 |
DOC_PP4_FxxP_1 | 175 | 178 | PF00568 | 0.395 |
DOC_PP4_FxxP_1 | 50 | 53 | PF00568 | 0.542 |
DOC_SPAK_OSR1_1 | 359 | 363 | PF12202 | 0.364 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.624 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.708 |
LIG_14-3-3_CanoR_1 | 126 | 134 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 185 | 190 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 210 | 218 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 7 | 11 | PF00244 | 0.546 |
LIG_BRCT_BRCA1_1 | 171 | 175 | PF00533 | 0.389 |
LIG_BRCT_BRCA1_1 | 86 | 90 | PF00533 | 0.501 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.423 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.387 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.425 |
LIG_FHA_2 | 135 | 141 | PF00498 | 0.574 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.432 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.541 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.385 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.367 |
LIG_LIR_Apic_2 | 172 | 178 | PF02991 | 0.391 |
LIG_LIR_Apic_2 | 49 | 53 | PF02991 | 0.534 |
LIG_LIR_Apic_2 | 64 | 68 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 230 | 240 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 268 | 276 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 268 | 272 | PF02991 | 0.317 |
LIG_SH2_CRK | 14 | 18 | PF00017 | 0.437 |
LIG_SH2_CRK | 65 | 69 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 171 | 175 | PF00017 | 0.275 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.300 |
LIG_SH2_STAP1 | 46 | 50 | PF00017 | 0.416 |
LIG_SH2_STAT3 | 151 | 154 | PF00017 | 0.473 |
LIG_SH2_STAT3 | 171 | 174 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.382 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.406 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.384 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.366 |
LIG_SUMO_SIM_par_1 | 165 | 173 | PF11976 | 0.491 |
LIG_SUMO_SIM_par_1 | 185 | 192 | PF11976 | 0.621 |
LIG_TRAF2_1 | 137 | 140 | PF00917 | 0.570 |
LIG_TRAF2_1 | 213 | 216 | PF00917 | 0.430 |
LIG_TRAF2_1 | 3 | 6 | PF00917 | 0.566 |
LIG_TRAF2_1 | 35 | 38 | PF00917 | 0.453 |
LIG_TYR_ITIM | 316 | 321 | PF00017 | 0.397 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.684 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.574 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.537 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.610 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.723 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.570 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.409 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.428 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.495 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.755 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.501 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.323 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.727 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.674 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.728 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.766 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.654 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.623 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.562 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.540 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.652 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.346 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.540 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.652 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.473 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.469 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.527 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.318 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.501 |
MOD_NEK2_2 | 13 | 18 | PF00069 | 0.567 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.741 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.438 |
MOD_PIKK_1 | 19 | 25 | PF00454 | 0.566 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.432 |
MOD_PKA_1 | 199 | 205 | PF00069 | 0.525 |
MOD_PKA_1 | 334 | 340 | PF00069 | 0.491 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.572 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.585 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.527 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.557 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.570 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.547 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.645 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.313 |
MOD_Plk_4 | 311 | 317 | PF00069 | 0.493 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.469 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.559 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.685 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.707 |
TRG_DiLeu_BaEn_1 | 6 | 11 | PF01217 | 0.443 |
TRG_DiLeu_BaEn_4 | 165 | 171 | PF01217 | 0.498 |
TRG_DiLeu_BaLyEn_6 | 129 | 134 | PF01217 | 0.550 |
TRG_DiLeu_BaLyEn_6 | 249 | 254 | PF01217 | 0.337 |
TRG_DiLeu_BaLyEn_6 | 55 | 60 | PF01217 | 0.456 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.418 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.699 |
TRG_ER_diArg_1 | 198 | 201 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 333 | 335 | PF00400 | 0.660 |
TRG_NLS_MonoExtN_4 | 196 | 202 | PF00514 | 0.589 |
TRG_Pf-PMV_PEXEL_1 | 210 | 215 | PF00026 | 0.475 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9D4 | Leptomonas seymouri | 69% | 99% |
A0A0S4IZI8 | Bodo saltans | 39% | 86% |
A0A1X0P7V3 | Trypanosomatidae | 45% | 100% |
A0A3R7K298 | Trypanosoma rangeli | 46% | 100% |
A0A3S7XAU7 | Leishmania donovani | 100% | 100% |
A4HP78 | Leishmania braziliensis | 88% | 100% |
D0A374 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9ASY6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q1L2 | Leishmania major | 93% | 100% |
V5DCI4 | Trypanosoma cruzi | 45% | 100% |